Join our team as a Lead SAS Programmer where you will contribute to impactful clinical trials by developing analysis datasets and leading programming efforts.

We're seeking a Senior Statistical Analyst with a strong background in SAS programming and at least three years of experience in a pharmaceutical or CRO environment. Your role will encompass validating ADaM datasets, creating productive standard macros, and communicating effectively with clients and stakeholders.

Key Responsibilities:
• Develop and validate ADaM datasets and TFLs using SAS
• Write, review, and maintain programming specifications
• Utilize standard macros to enhance programming workflows
• Lead project timelines and guide junior team members
• Conduct code reviews to ensure high-quality outputs

Requirements:
• Bachelor's degree in Statistics, Mathematics, or similar field
• Minimum 3 years SAS programming experience in relevant settings
• Strong understanding of clinical trial requirements
• Proven experience in leading programming projects
• Excellent global communication abilities

Leverage your SAS expertise and leadership to drive excellence in statistical analysis.
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📌 Lead SAS Programmer - Senior Statistical Analyst (Nova Scotia)
🏢 Bilinguallink
📍 Nova Scotia